EP0066552A1 - Procédé pour déterminer la concentration de créatinine dans des liquides biologiques et réactif pour réaliser ce procédé - Google Patents

Procédé pour déterminer la concentration de créatinine dans des liquides biologiques et réactif pour réaliser ce procédé Download PDF

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Publication number
EP0066552A1
EP0066552A1 EP82830126A EP82830126A EP0066552A1 EP 0066552 A1 EP0066552 A1 EP 0066552A1 EP 82830126 A EP82830126 A EP 82830126A EP 82830126 A EP82830126 A EP 82830126A EP 0066552 A1 EP0066552 A1 EP 0066552A1
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EP
European Patent Office
Prior art keywords
creatinine
hydrogen peroxide
peroxydasis
determining
consist
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP82830126A
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German (de)
English (en)
Inventor
Giorgio Torelli
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Chemical Laboratories Srl
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Chemical Laboratories Srl
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Publication date
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Publication of EP0066552A1 publication Critical patent/EP0066552A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/34—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/70—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving creatine or creatinine

Definitions

  • the present invention relates to a method for determining the creatinine contents in biological liquids and to a reagent for carrying out the method.
  • the creatinine contents in biological liquids is conventionally determined by means of the Jaffé reaction (see Jaffé M-Zschr.-Physiol Chem.10.391 1886) which is based on the creatinine property of reducing the picric and picramic acids in an alkaly solution and providing a red-orange solution.More specifically the concentration of the reaction product is determined by colorimetry at a wave length of about 510nm. The analysis can be carried out at equilibrium conditions (end point) either by means of a preliminary deproteinizing step or without using any steps of this type,and under kinetic conditions (rixed time) without any deproteinizing steps.
  • a drawback which is common to all of these methods is the inherent lack of specificity of the chemical process,since the reduction or picric acid to picramic acid is not a characteristic peculiar to creatinine and, therefore, it may also be caused by other substances present in biological liquids, such as many metabolism compounds related to creatinine.
  • the task or the present invention is to obviate the mentioned drawback by providing a new method for determining the creatinine contents or concentration in biological liquids effective to allow for a high reaction specificity to be obtained as well as highly reliable results about the creatinine amount contained in said biological liquids.
  • Yet another object of the present invention is to provide a method for determining the creatinine contents or concentration in biological liquids effective to give a high reproductibility of the analytical data.
  • Yet another object of the present invention is to provide a reagent for determining the creatinine contents or concentration in biological liquids which is effective to carry out the above mentioned method.
  • a method for determining the creatinine contents or concentration in biological liquids characterized in that it comprises the steps or enzymatically transforming creatinine to glycine,acetaldehyde and hydrogen peroxide and proportioning one of the reaction end products.
  • the proportioned product is the hydrogen peroxide,which is proportioned by using a conventional proportioning method,such as titration,potentiometric methods,colorimetric methods or enzymatic methods or the like.
  • said hydrogen peroxide is enzymatically proportioned,by using catalasis or peroxydasis in the presence of compounds effective to provide a chromogen compound which is colorimetrically analyzed.
  • the enzymes used in the instant method for determining the creatinine contents or concentration consist of the creatinine- amiaonyarolasis effective to transform creatinine into creatine oy addition of water,tne creatineamidohydrolasis effective to transform creatine into urea and sarcosine by aadition of water and the sarcosineoxydasis which, also by addition of water, is effective to transform sarcosine into glycine,acetaldebyde and hydrogen peroxide.
  • the compounds effective to provide a chromogen compouna upon catalasis or peroxydasis are 4-aminophenazone and the like, phenol and the halogenated derivavives thereof, or aromatic amines.
  • the reagent preferably comprises a phosphate buffer,aminoantipirine,dichlorophenolsulphonate, creatinineamidohydrolasis, creatineamidohydrolasis, sarcosineoxydasis ana peroxydasis.
  • the hydrogen peroxide amount for example by using conventional quantitative analytical methods, such as titration, potentiometric procedures, colorimetric and enzymatic methods and so on.
  • the most preferred way is the enzymatic procedure,by using catalasis or peroxydasis which, in the presence of 4-aminophenazone or the like, phenol and halogenated derivatives thereof, aromatic amines,are effective to provide a chromogen compound having a maximum at about 510nm.
  • These reactions are generally indicated as of the "Trinder” type (see Trinder P.J.Clin.Pat.22.158 (1969) ).
  • aniline dimethylanillne, diethylaniline have been found to be particularly effective.
  • a particularly effective method for determining the hydrogen peroxide amount is that exploiting the property of said hydrogen peroxide or oxidizing iodides,such as potassium iodide,to iodine which is determined colorimetrically at 365 or 405nm (or by filters near to this wavelenght).
  • oxidizing iodides such as potassium iodide,to iodine which is determined colorimetrically at 365 or 405nm (or by filters near to this wavelenght).
  • a very effective method for determining the H202 amount is obtained by the action of peroxidasis on a mixture of 3 hydroxy 2-4-6-tri- iodine benzoic acid and 3-methyl-benzothioazoline- hydrazone-hydrochloride monohydrate.
  • the phosphate buffer may consist of 12g/l of monopotassium phosphate,19.5 g/1 of bipotassium phosphate, 4g/l of tetrasodium EDTA and 5g/l of triton-100.
  • the mixture is introduced into a thermostat adjusted at 37°C for 45 minutes and a read out is performed at 560 nm against the respective blanks obtainea by diluting 50 ⁇ l of standard and samples with the same reagent with the exception that the latter did not contain creatinineamidohydrolasis.
  • the sample creatinine is calculated by using the following formula:
  • the methods according to the invention allows for a great reaction specificity to be obtained by using a single reactive, which permits to easily mechanize the proceaure and affords highly reproaucible aata.ln addition to the foregoing,as it will be clear from the graph of fig.1, the advantage is obtained of having a linear reaction up to a creatinine concentration of 8mg/dl, which value is an effectively suitable one for the examined creatinine containing biological liquids.
  • Another advantage consists of the standard reproductibility which,as carried out on 20 samples,has been found to be of 2.9%, while the serum reproductibility,also on 20 samples,was of 4.1%.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • Food Science & Technology (AREA)
  • Cell Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
EP82830126A 1981-05-28 1982-05-10 Procédé pour déterminer la concentration de créatinine dans des liquides biologiques et réactif pour réaliser ce procédé Withdrawn EP0066552A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT22009/81A IT1137075B (it) 1981-05-28 1981-05-28 Procedimento per la determinazione della creattinina (creatininio) in liquidi biologici, e reattivo per la sua attuazione
IT2200981 1981-05-28

Publications (1)

Publication Number Publication Date
EP0066552A1 true EP0066552A1 (fr) 1982-12-08

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EP82830126A Withdrawn EP0066552A1 (fr) 1981-05-28 1982-05-10 Procédé pour déterminer la concentration de créatinine dans des liquides biologiques et réactif pour réaliser ce procédé

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EP (1) EP0066552A1 (fr)
IT (1) IT1137075B (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0112571A1 (fr) * 1982-12-27 1984-07-04 Roche Diagnostics GmbH Procédé et réactif pour la détermination de la N-carbamoylsarcosine et une enzyme pour ce procédé
EP0201805A1 (fr) * 1985-04-30 1986-11-20 Roche Diagnostics GmbH Préparation stabilisée de sarcosine oxydase
GB2185318A (en) * 1986-01-14 1987-07-15 Genetics Int Inc Creatinine assay
US4816393A (en) * 1984-02-24 1989-03-28 Boehringer Mannheim Gmbh Nucleoside triphosphate-dependent 1-methylhydantoinase, a process for obtaining it and the use thereof
CN106645758A (zh) * 2017-01-03 2017-05-10 长沙中生众捷生物技术有限公司 肌酐的检测试剂及肌酐的检测试纸
WO2021086209A1 (fr) * 2019-10-30 2021-05-06 Uniwersytet Warszawski Procédé analytique fluorométrique pour la détermination de la créatinine dans des échantillons biologiques cliniquement significatifs et réactif fluorométrique destiné à être utilisé dans ce procédé
US11874285B2 (en) 2014-12-18 2024-01-16 Radiometer Medical Aps Method for calibrating a device for measuring the concentration of creatinine

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3003490A1 (de) * 1979-01-31 1980-08-14 Millipore Corp Reagenz zur analytischen bestimmung von wasserstoffperoxid
EP0033462A1 (fr) * 1980-02-04 1981-08-12 ELVI S.p.A. Réactif de Trinder amélioré par l'aminopyrine et procédé de dosage du peroxyde d'hydrogène produit par oxydation enzymatique de substrats métaboliques, à l'aide de ce réactif

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3003490A1 (de) * 1979-01-31 1980-08-14 Millipore Corp Reagenz zur analytischen bestimmung von wasserstoffperoxid
EP0033462A1 (fr) * 1980-02-04 1981-08-12 ELVI S.p.A. Réactif de Trinder amélioré par l'aminopyrine et procédé de dosage du peroxyde d'hydrogène produit par oxydation enzymatique de substrats métaboliques, à l'aide de ce réactif

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CHEMICAL AND PHARMACEUTICAL BULLETIN, Vol. 28, No. 12, 1980, Tokyo, T. KINOSHITA et al. "A Fluorophotometric Determination of Serum Creatinine and Creatine using a Creatinineamidohydrolase-Creatineamidinohydrolase-Sarcosine Oxidase-Peroxidase System and Diacetyldichlorofluorescin" pages 3501 to 3506 *
JOURNAL OF ANALYTICAL CHEMISTRY OF U.S.S.R., Vol. 35, No. 8, Part 2, August 1980, New York, I.F. DOLMANOVA et al. "Enzymatic Methods of Analysis" pages 1042 to 1081 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0112571A1 (fr) * 1982-12-27 1984-07-04 Roche Diagnostics GmbH Procédé et réactif pour la détermination de la N-carbamoylsarcosine et une enzyme pour ce procédé
US4816393A (en) * 1984-02-24 1989-03-28 Boehringer Mannheim Gmbh Nucleoside triphosphate-dependent 1-methylhydantoinase, a process for obtaining it and the use thereof
EP0201805A1 (fr) * 1985-04-30 1986-11-20 Roche Diagnostics GmbH Préparation stabilisée de sarcosine oxydase
GB2185318A (en) * 1986-01-14 1987-07-15 Genetics Int Inc Creatinine assay
US11874285B2 (en) 2014-12-18 2024-01-16 Radiometer Medical Aps Method for calibrating a device for measuring the concentration of creatinine
CN106645758A (zh) * 2017-01-03 2017-05-10 长沙中生众捷生物技术有限公司 肌酐的检测试剂及肌酐的检测试纸
WO2021086209A1 (fr) * 2019-10-30 2021-05-06 Uniwersytet Warszawski Procédé analytique fluorométrique pour la détermination de la créatinine dans des échantillons biologiques cliniquement significatifs et réactif fluorométrique destiné à être utilisé dans ce procédé

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Publication number Publication date
IT1137075B (it) 1986-09-03
IT8122009A0 (it) 1981-05-28

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Inventor name: TORELLI, GIORGIO